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macular degeneration/hovedpine
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Dengue maculopathy: a case report.
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BACKGROUND
Dengue fever is endemic in many countries of South East Asia. In spite of the occasional epidemics, dengue maculopathy remains a rare entity.
METHODS
A 31-year-old gentleman was admitted with a 6-day history of fever, generalised rash, headache and myalgia after a trip to Malaysia. There
A double-blind placebo-controlled evaluation of the acute effects of sildenafil citrate (Viagra) on visual function in subjects with early-stage age-related macular degeneration.
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OBJECTIVE
To assess the effects of a single 100-mg dose of sildenafil citrate on visual function in men with early-stage age-related macular degeneration.
METHODS
Randomized double-blind placebo-controlled clinical trial.
METHODS
Nine men (mean age 71 years, range 59-85 years) with early-stage
Persistent Placoid Maculopathy Complicated by Cerebral Vasculitis.
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Persistent placoid maculopathy (PPM) is a bilateral inflammatory chorioretinopathy characterized by long-standing plaque-like macular lesions. No systemic manifestations have been reported to date. We describe a case of PPM complicated by cerebral vasculitis, suggesting that neurological symptoms,
Vascular disrupting agent for neovascular age related macular degeneration: a pilot study of the safety and efficacy of intravenous combretastatin A-4 phosphate.
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BACKGROUND
This study was designed to assess the safety, tolerability, and efficacy of intravenous infusion of CA4P in patients with neovascular age-related macular degeneration (AMD).
METHODS
Prospective, interventional, dose-escalation clinical trial. Eight patients with neovascular AMD refractory
Spontaneous suprachoroidal hemorrhage associated with age-related macular degeneration and anticoagulation therapy.
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Suprachoroidal hemorrhage is a rare but dreadful event. We report the case of an 86-year-old man with age-related macular degeneration (ARMD) in both eyes. He had been receiving anticoagulation therapy for several years for systemic disease. He presented with severe headache and intractable pain in
OCT Angiography of Paracentral Acute Middle Maculopathy Associated With Central Retinal Artery Occlusion and Deep Capillary Ischemia.
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An 82-year-old man presented with acute, painless vision loss in the left eye associated with headaches, jaw claudication, and scalp tenderness. Clinical examination and fluorescein angiography confirmed the diagnosis of a central retinal artery occlusion of the left eye. Spectral-domain optical
Refractory Giant Cell Arteritis Complicated by Vision Loss From Optic Atrophy and Maculopathy Associated With Pachymeningitis.
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BACKGROUND
We describe a 75-year-old woman who experienced vision loss in her left eye due to biopsy-proven giant cell arteritis (GCA). She subsequently developed pachymeningitis causing refractory headaches and bilateral optic neuropathy and maculopathy.
METHODS
Case report with literature
Bull's eye maculopathy associated with hereditary hemochromatosis.
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Purpose
To report a case of bull's eye maculopathy, a novel finding in a patient with iron overload secondary to hereditary hemochromatosis with a homozygous mutation of the HFE gene.Dengue related maculopathy and foveolitis.
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A 24 year-old Malay lady presented with high grade fever, myalgia, generalized rashes, severe headache and was positive for dengue serology test. Her lowest platelet count was 45 × 10(9) cells/L. She complained of sudden onset of painlessness, profound loss of vision bilaterally 7 days after the
Acupuncture benefits for Flammer syndrome in individuals with inherited diseases of the retina.
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BACKGROUND
Patients with inherited diseases of the retina (IRD) often exhibit signs and symptoms of Flammer syndrome (FS). Acupuncture treatment has shown its positive effect on visual function in patients with IRD. The aim of the present study is to examine the effect of acupuncture on signs and
Variable retinal and neurologic manifestations in patients harboring the mitochondrial DNA 8993 mutation.
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OBJECTIVE
Ophthalmologic and neurologic manifestations of the mitochondrial DNA mutation at position 8993 (MTATP*NARP8993) are reported and compared with previously published reports of patients with the 8993 mutation and other mitochondrial disorders.
METHODS
Pedigree analysis.
METHODS
University
Ocular imaging findings of bilateral optic disc pit in a child.
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BACKGROUND
To report a rare condition of bilateral optic disc pit in a child.
METHODS
A ten-year-old female was admitted with a complaint of headache. Visual acuity was 20/20 in both eyes (OU). Anterior segment examination was normal in OU. Fundus examination revealed optic disc pit (ODP) located
[Cryptococcal chorioretinitis and acquired immunodeficiency syndrome: apropos of a case].
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A patient with acquired immune deficiency and antecedents of pancreatitis presented with headaches, fever, dyspnea and bilateral decrease of vision. A diagnosis of disseminated cryptococcosis was made by lumbar puncture, alveolar washing and elevated cryptococcal antigen in blood, urine and stool.
Retinal pigment epithelium tear as a cause of vitreous hemorrhage.
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Tearing of the retinal pigment epithelium (RPE) can complicate its detachment in the course of senile macular degeneration. In the majority of cases, there is progression to the formation of a macular fibrous scar with poor visual outcome. There have not been any previous reports of vitreous
[Treatment of serous macular retinal detachment with antihistamines].
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The etiology of retinal detachment in central serous retinopathy (CSR) is unknown; however, three facts are generally accepted: (1) the serous exudate which raises the layers of the receptors/pigment epithelium is formed due to hyperpermeability in the choriocapillaries, (2) patients frequently
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